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Work Background
ICON plcSenior Clinical Research Associate
Mar. 2022 - Apr. 2025United States
IQVIASenior Clinical Research Associate
Jun. 2021 - Mar. 2022Houston, Texas, United States Performing site selection, initiation, monitoring, and close-out visits, plus maintaining appropriate documentation Supporting the development of a subject recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
DOCSClinical Research Associate
Jan. 2020 - May. 2021United States• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products and/or medical devices.
• Conduct site visits to determine protocol and regulatory compliance, and prepared required documentation
• Develop collaborative relationships with investigative sites, client company personnel and study vendors
• Perform Site Initiation Visits and Routine/Interim Monitoring Visits
• Perform risk based monitoring duties for participating protocols
• Report writing
• Upload essential documents and navigate the electronic trial master file
PPDClinical Research Associate
Dec. 2018 - Nov. 2019• Attend sponsor calls and internal team calls to stay informed of current study issues
• Perform and coordinate assigned aspects of the clinical monitoring process in accordance with GCPs and global SOPs to assess the safety and efficacy of investigational products and/or medical devices.
• Conduct site visits to determine protocol and regulatory compliance, and prepared required documentation
• Develop collaborative relationships with investigative sites, client company personnel and study vendors
• Complete site selection procedures prior to study start up (Feasibility).
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